14591
|
|
|
VOPP1 WW domain binding protein |
ECOP, GASP, WBP1L2 |
|
14592
|
|
|
V-set pre-B cell surrogate light chain 1 |
CD179a, IGI, IGVPB, VPREB |
|
14593
|
|
|
VPS11 core subunit of CORVET and HOPS complexes |
DYT32, END1, HLD12, HLD12; DYT32, PEP5, RNF108, hVPS11 |
|
14594
|
|
|
Vacuolar protein sorting 13 homolog A |
BLTP5A, CHAC, CHOREIN |
|
14595
|
|
|
Vacuolar protein sorting 13 homolog B |
BLTP5B, CHS1, COH1 |
Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Cholecystolithiasis, Ciliary dyskinesia, Cohen syndrome, Congenital neurologic anomalies, Dental caries, Endometriosis, Long qt syndrome, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Lung cancer, Meniere disease, Myopia, Pituitary stalk interruption syndrome, Retinitis pigmentosa, Schizophrenia, Squamous cell carcinoma, UrolithiasisView all (7 more) |
14596
|
|
|
Vacuolar protein sorting 13 homolog C |
BLTP5C, PARK23 |
Parkinson disease, Bipolar disorder, Diabetic retinopathy, Hemiparkinsonism, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Alzheimer disease, Schizophrenia, Thyroid hemiagenesis, Diabetes mellitus type 2 |
14597
|
|
|
Vacuolar protein sorting 13 homolog D |
BLTP5D, SCA24, SCAR4, SCASI |
Arthrogryposis multiplex congenita, Spinocerebellar ataxia, Cerebellar ataxia, Central nervous system cancer, Cholecystolithiasis, Glioblastoma, Glioma, Non-immune hydrops fetalis, Leigh syndrome, Neurodevelopmental disorder, Pena-shokeir syndrome , Psychiatric disorders |
14598
|
|
|
VPS16 core subunit of CORVET and HOPS complexes |
DYT30, hVPS16 |
|
14599
|
|
|
VPS18 core subunit of CORVET and HOPS complexes |
PEP3 |
|
14600
|
|
|
VPS26 retromer complex component A |
HB58, Hbeta58, PEP8A, VPS26 |
|